Cell Receptor and Cofactor Interactions of the Contact Activation System and Factor XI

The contact activation system (CAS) or contact pathway is central to the crosstalk between coagulation and inflammation and contributes to diverse disorders affecting the cardiovascular system. CAS initiation contributes to thrombosis but is not required for hemostasis and can trigger plasma coagula...

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Main Authors: Monika Pathak, Bubacarr Gibril Kaira, Alexandre Slater, Jonas Emsley
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Medicine
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fmed.2018.00066/full
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author Monika Pathak
Bubacarr Gibril Kaira
Alexandre Slater
Jonas Emsley
author_facet Monika Pathak
Bubacarr Gibril Kaira
Alexandre Slater
Jonas Emsley
author_sort Monika Pathak
collection DOAJ
description The contact activation system (CAS) or contact pathway is central to the crosstalk between coagulation and inflammation and contributes to diverse disorders affecting the cardiovascular system. CAS initiation contributes to thrombosis but is not required for hemostasis and can trigger plasma coagulation via the intrinsic pathway [through factor XI (FXI)] and inflammation via bradykinin release. Activation of factor XII (FXII) is the principal starting point for the cascade of proteolytic cleavages involving FXI, prekallikrein (PK), and cofactor high molecular weight kininogen (HK) but the precise location and cell receptor interactions controlling these reactions remains unclear. FXII, PK, FXI, and HK utilize key protein domains to mediate binding interactions to cognate cell receptors and diverse ligands, which regulates protease activation. The assembly of contact factors has been demonstrated on the cell membranes of a variety of cell types and microorganisms. The cooperation between the contact factors and endothelial cells, platelets, and leukocytes contributes to pathways driving thrombosis yet the basis of these interactions and the relationship with activation of the contact factors remains undefined. This review focuses on cell receptor interactions of contact proteins and FXI to develop a cell-based model for the regulation of contact activation.
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spelling doaj.art-ed20c7fe7bd14b2db144fe37597d9c8d2022-12-22T02:42:41ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2018-03-01510.3389/fmed.2018.00066337964Cell Receptor and Cofactor Interactions of the Contact Activation System and Factor XIMonika Pathak0Bubacarr Gibril Kaira1Alexandre Slater2Jonas Emsley3Centre for Biomolecular Sciences, School of Pharmacy, University of Nottingham, Nottingham, United KingdomCentre for Biomolecular Sciences, School of Pharmacy, University of Nottingham, Nottingham, United KingdomCentre for Biomolecular Sciences, School of Pharmacy, University of Nottingham, Nottingham, United KingdomCentre for Biomolecular Sciences, School of Pharmacy, University of Nottingham, Nottingham, United KingdomThe contact activation system (CAS) or contact pathway is central to the crosstalk between coagulation and inflammation and contributes to diverse disorders affecting the cardiovascular system. CAS initiation contributes to thrombosis but is not required for hemostasis and can trigger plasma coagulation via the intrinsic pathway [through factor XI (FXI)] and inflammation via bradykinin release. Activation of factor XII (FXII) is the principal starting point for the cascade of proteolytic cleavages involving FXI, prekallikrein (PK), and cofactor high molecular weight kininogen (HK) but the precise location and cell receptor interactions controlling these reactions remains unclear. FXII, PK, FXI, and HK utilize key protein domains to mediate binding interactions to cognate cell receptors and diverse ligands, which regulates protease activation. The assembly of contact factors has been demonstrated on the cell membranes of a variety of cell types and microorganisms. The cooperation between the contact factors and endothelial cells, platelets, and leukocytes contributes to pathways driving thrombosis yet the basis of these interactions and the relationship with activation of the contact factors remains undefined. This review focuses on cell receptor interactions of contact proteins and FXI to develop a cell-based model for the regulation of contact activation.http://journal.frontiersin.org/article/10.3389/fmed.2018.00066/fullcontact activation systemfactor XIIfactor XIplasma kallikreinhigh molecular weight kininogenendothelial cell
spellingShingle Monika Pathak
Bubacarr Gibril Kaira
Alexandre Slater
Jonas Emsley
Cell Receptor and Cofactor Interactions of the Contact Activation System and Factor XI
Frontiers in Medicine
contact activation system
factor XII
factor XI
plasma kallikrein
high molecular weight kininogen
endothelial cell
title Cell Receptor and Cofactor Interactions of the Contact Activation System and Factor XI
title_full Cell Receptor and Cofactor Interactions of the Contact Activation System and Factor XI
title_fullStr Cell Receptor and Cofactor Interactions of the Contact Activation System and Factor XI
title_full_unstemmed Cell Receptor and Cofactor Interactions of the Contact Activation System and Factor XI
title_short Cell Receptor and Cofactor Interactions of the Contact Activation System and Factor XI
title_sort cell receptor and cofactor interactions of the contact activation system and factor xi
topic contact activation system
factor XII
factor XI
plasma kallikrein
high molecular weight kininogen
endothelial cell
url http://journal.frontiersin.org/article/10.3389/fmed.2018.00066/full
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AT bubacarrgibrilkaira cellreceptorandcofactorinteractionsofthecontactactivationsystemandfactorxi
AT alexandreslater cellreceptorandcofactorinteractionsofthecontactactivationsystemandfactorxi
AT jonasemsley cellreceptorandcofactorinteractionsofthecontactactivationsystemandfactorxi